Canonical Allele Identifier: CA408710476

Gene: PROCR

Linked Data

• gnomAD v4: 20-35176697-G-A
• MyVariant Identifiers: chr20:g.33764500G>A (hg19) ; chr20:g.35176697G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35176697G>A , CM000682.2:g.35176697G>A	GRCh38
NC_000020.10:g.33764500G>A , CM000682.1:g.33764500G>A	GRCh37
NC_000020.9:g.33228161G>A	NCBI36
NG_032899.1:g.9727G>A
NG_032899.2:g.9727G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216968.5:c.602-1G>A MANE Select	ENSP00000216968.3:n.602-1G>A
ENST00000216968.4:c.602-1G>A	ENSP00000216968.3:n.602-1G>A
ENST00000634509.1:c.94+251G>A	ENSP00000489456.1:n.94+251G>A
ENST00000635377.1:c.501+251G>A
NM_006404.4:c.602-1G>A	NP_006395.2:n.602-1G>A
XM_011528496.1:c.601+251G>A	XP_011526798.1:n.601+251G>A
NM_001355008.1:c.-101-10826C>T	NP_001341937.1:n.-101-10826C>T
NM_006404.5:c.602-1G>A MANE Select	NP_006395.2:n.602-1G>A
NM_001355008.2:c.-101-10826C>T	NP_001341937.1:n.-101-10826C>T